ENST00000327946.12:c.1233+5965T>A
MANE Select
|
ENSP00000330148.7:n.1233+5965T>A
|
|
ENST00000327946.11:c.1233+5965T>A
|
ENSP00000330148.7:n.1233+5965T>A
|
|
ENST00000464741.2:c.1233+5965T>A
|
ENSP00000433064.1:n.1233+5965T>A
|
|
ENST00000536331.5:c.453+5965T>A
|
ENSP00000444455.2:n.453+5965T>A
|
|
NM_017551.2:c.1233+5965T>A
|
NP_060021.1:n.1233+5965T>A
|
|
XM_011539720.1:c.1233+5965T>A
|
XP_011538022.1:n.1233+5965T>A
|
|
XM_011539720.2:c.1233+5965T>A
|
XP_011538022.1:n.1233+5965T>A
|
|
NM_017551.3:c.1233+5965T>A
MANE Select
|
NP_060021.1:n.1233+5965T>A
|
|